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Showing results (31-40 of 70) with videos related to

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American Journal of Human Genetics|June 1, 1997
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codonG Stevanin, A S Lebre, C Mathieux, et al.
European Urology|September 18, 2002
A candidate gene approach within the susceptibility region PCaP on 1q42.2-43 excludes deleterious mutations of the PCTA-1 gene to be responsible for hereditary prostate cancerC Maier, K Rösch, K Herkommer, et al.
Neurology|December 31, 1997
Clinical and molecular features of spinocerebellar ataxia type 6G Stevanin, A Dürr, G David, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 25, 2025
Differential Validity in the Written, Oral, and Electronic SDMT in Multiple SclerosisMatthew A Greenwald, Héctor G Cancel Asencio, Jenifer Dwyer, et al.
American Journal of Human Genetics|October 1, 1995
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locusG Cancel, N Abbas, G Stevanin, et al.
Brain : a Journal of Neurology|December 1, 1995
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 familiesA Dürr, D Smadja, G Cancel, et al.
Neuroreport|July 17, 1998
Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onsetI Gourfinkel-An, G Cancel, C Duyckaerts, et al.
American Journal of Human Genetics|January 1, 1994
A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusG Stevanin, E Le Guern, N Ravisé, et al.
Bulletin Du Cancer|January 12, 2011
[Strategies for early diagnosis and prevention of prostate cancer]A Valeri, B Malavaud, O Desrichard, et al.
Neurology|August 1, 1994
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.
Pageof 7

Showing results (31-40 of 70) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|June 1, 1997
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codonG Stevanin, A S Lebre, C Mathieux, et al.
European Urology|September 18, 2002
A candidate gene approach within the susceptibility region PCaP on 1q42.2-43 excludes deleterious mutations of the PCTA-1 gene to be responsible for hereditary prostate cancerC Maier, K Rösch, K Herkommer, et al.
Neurology|December 31, 1997
Clinical and molecular features of spinocerebellar ataxia type 6G Stevanin, A Dürr, G David, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|April 25, 2025
Differential Validity in the Written, Oral, and Electronic SDMT in Multiple SclerosisMatthew A Greenwald, Héctor G Cancel Asencio, Jenifer Dwyer, et al.
American Journal of Human Genetics|October 1, 1995
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locusG Cancel, N Abbas, G Stevanin, et al.
Brain : a Journal of Neurology|December 1, 1995
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 familiesA Dürr, D Smadja, G Cancel, et al.
Neuroreport|July 17, 1998
Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onsetI Gourfinkel-An, G Cancel, C Duyckaerts, et al.
American Journal of Human Genetics|January 1, 1994
A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusG Stevanin, E Le Guern, N Ravisé, et al.
Bulletin Du Cancer|January 12, 2011
[Strategies for early diagnosis and prevention of prostate cancer]A Valeri, B Malavaud, O Desrichard, et al.
Neurology|August 1, 1994
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.
Pageof 7